A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053520



Internal ID21962753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43679201..43679791hg38UCSC Ensembl
chr19:44183353..44183943hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053520
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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